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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 56349Generated: October 25, 2026

3-methyl-1-phenyl-1H-pyrazole-5-carboxylic acid → 1-(4-Fluoro-phenyl)-2-[4-(5-methyl-2-phenyl-2H-pyrazole-3-carbonyl)-piperazin-1-yl]-ethanone

https://huagongshe.com/reaction/56349

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-methyl-1-phenyl-1H-pyrazole-5-carboxylic acidHCID 2769592—
Reactant1-(4-Fluorophenyl)-2-(piperazin-1-yl)ethan-1-one dihydrochlorideHCID 42933716—
Product1-(4-Fluoro-phenyl)-2-[4-(5-methyl-2-phenyl-2H-pyrazole-3-carbonyl)-piperazin-1-yl]-ethanoneHCID 2481117978.5%

Reaction Steps

The title compound was prepared in a similar manner as described in Example 1.2, using 3-methyl-1-phenyl-1H-pyrazole-5-carboxylic acid (30.3 mg), and 1-(4-fluorophenyl)-2-(piperazin-1-yl)ethanone dihydrochloride (29.5 mg) as starting materials, to afford the title compound (31.9 mg) as a white solid. 1H NMR (400 MHz, CDCl3) δ 2.35 (s, 3H), 2.60-2.67 (m, 2H), 2.69 (bs., 2H), 3.81 (s, 2H), 3.89 (bs, 2H), 4.16 (bs, 2H), 6.62 (s, 1H), 7.13 (t, J=8.46 Hz, 2H), 7.38-7.54 (m, 5H), 7.99-8.09 (m, 2H). Exact mass calculated for C23H23FN4O2: 406.2. Found: LCMS m/z=407.5 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434692B2
Source datasetuspto-grants-2016_09
ORD IDord-5c7489a207554188911e22e887092d9d
Source noteuspto-grants-2016_09